Variant report
Variant | rs73745876 |
---|---|
Chromosome Location | chr6:69515259-69515260 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
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No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr6:69513585..69517599-chr6:69517600..69520512,4 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs55792962 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55840344 | 0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55867330 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs55915457 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs56075259 | 1.00[EUR][1000 genomes] |
rs56236762 | 1.00[EUR][1000 genomes] |
rs56998424 | 0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58108540 | 0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs59310513 | 1.00[EUR][1000 genomes] |
rs59384052 | 1.00[EUR][1000 genomes] |
rs59877292 | 1.00[EUR][1000 genomes] |
rs60607705 | 1.00[EUR][1000 genomes] |
rs60892917 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs60923857 | 1.00[EUR][1000 genomes] |
rs6910603 | 1.00[EUR][1000 genomes] |
rs73463925 | 0.88[EUR][1000 genomes] |
rs73463928 | 0.88[EUR][1000 genomes] |
rs73463932 | 0.94[EUR][1000 genomes] |
rs73463934 | 1.00[EUR][1000 genomes] |
rs73463935 | 1.00[EUR][1000 genomes] |
rs73463941 | 0.94[EUR][1000 genomes] |
rs73463946 | 1.00[EUR][1000 genomes] |
rs73463952 | 1.00[EUR][1000 genomes] |
rs73467839 | 1.00[EUR][1000 genomes] |
rs73467848 | 1.00[EUR][1000 genomes] |
rs73467883 | 1.00[EUR][1000 genomes] |
rs73467884 | 1.00[EUR][1000 genomes] |
rs73745828 | 0.94[EUR][1000 genomes] |
rs73745858 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745859 | 0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745860 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745861 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745863 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745866 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745867 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745870 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745879 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745880 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs73745881 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv886130 | chr6:68950298-69531957 | Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
2 | nsv886131 | chr6:69480628-69545903 | Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
3 | nsv886132 | chr6:69487204-69610281 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer | Chromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1017659 | chr6:69489481-69520127 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:69505600-69522800 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
2 | chr6:69505600-69536000 | Weak transcription | Brain Inferior Temporal Lobe | brain |
3 | chr6:69510000-69525000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |